Meditech International Inc
Toronto Ontario, CA
Meditech International Inc appears in FDA device records in Toronto Ontario, CA. FDA records list 5 510(k) clearances between and , no PMA records and one registered establishment. As of , FDA records show no recalls for this company, and at least one establishment registration is current.
FDA records held for this company
510(k) clearance history
FDA records hold 5 510(k) clearances for Meditech International Inc between 2003 and 2008. The busiest year on record is 2008, with 2. The most recent is 2008, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2003 | 1 |
| 2005 | 1 |
| 2006 | 1 |
| 2008 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K081355 | BIOFLEX LD-R100 TREATMENT HEAD | ILY | Substantially Equivalent | |
| K072551 | LD-I 75 AND LD-I 200 | NHN | Substantially Equivalent | |
| K051875 | BIOFLEX PRESCRIPTION SYSTEM AND RELATED TREATMENT HEADS | ILY | Substantially Equivalent | |
| K041885 | BIOFLEX LD-175 AND LD-1200 TREATMENT HEADS | ILY | Substantially Equivalent | |
| K023621 | BIOFLEX PROFESSIONAL THERAPY SYSTEM | ILY | Substantially Equivalent |
Registered establishments
| Registration | FEI | Establishment | Address | Registration expires | Product codes listed |
|---|---|---|---|---|---|
| 3003082988 | 3003082988 | Meditech International Inc | 411 Horner Ave Unit 1, Toronto Ontario M8W 4W3 CA | 2026 |
Registration numbers link to the FDA registration and listing record for that establishment.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain